Osteogenesis imperfecta type 11

MONDO:0012592

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the FKBP10 gene.

Also known as: FKBP10 osteogenesis imperfecta, OI11, osteogenesis imperfecta caused by mutation in FKBP10, OI type 11, OI type XI, OI, type 11, osteogenesis imperfecta, type 11, osteogenesis imperfecta, type XI

0 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta type 11 itself.

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Part of

↑ Osteogenesis imperfecta and a reduction of bone mineral density. (307)

Including sub-types (0) Tagged with Osteogenesis imperfecta type 11 (0)

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